Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractA C. elegans male pheromone feminizes germline gene expression in hermaphrodites and imposes life-history costs    Next AbstractCross-kingdom effects of plant-plant signaling via volatile organic compounds emitted by tomato (Solanum lycopersicum) plants infested by the greenhouse whitefly (Trialeurodes vaporariorum) »

J Ethnopharmacol


Title:Antinociceptive effect of extracts and compounds from Hofmeisteria schaffneri
Author(s):Angeles-Lopez G; Perez-Vasquez A; Hernandez-Luis F; Deciga-Campos M; Bye R; Linares E; Mata R;
Address:"Departamento de Farmacia, Facultad de Quimica, Universidad Nacional Autonoma de Mexico, DF, Mexico"
Journal Title:J Ethnopharmacol
Year:2010
Volume:20100713
Issue:2
Page Number:425 - 432
DOI: 10.1016/j.jep.2010.07.009
ISSN/ISBN:1872-7573 (Electronic) 0378-8741 (Linking)
Abstract:"ETHNOPHARMACOLOGICAL RELEVANCE: Hofmeisteria schaffneri (Asteraceae) is a medicinal plant widely commercialized in the most important Markets of Mexico City for the treatment of gastro-intestinal complaints and skin afflictions. AIM OF THE STUDY: The main goals of this study were to establish the potential acute toxicity and the antinociceptive activity in animal models of several preparations and compounds from Hofmeisteria schaffneri. MATERIALS AND METHODS: The aqueous and organic extracts as well as the essential oil of Hofmeisteria schaffneri were prepared by infusion, maceration and hydrodistillation, respectively. Investigation of the acute toxicity was accomplished by the Lorke method. The antinociceptive effect was assessed using the writhing and the hot plate tests. Natural compounds were isolated by standard phytochemical procedures. In addition, a few thymol esters were prepared by chemical synthesis. The stability of natural and synthetic esters was qualitatively analyzed by measuring their susceptibility to hydrolysis by pig liver estearase and mouse plasma at 37 degrees C. RESULTS: The LD(50) for each preparation tested was higher than 5000 mg/kg revealing that they were not toxic to mice after exposure for short space of time. On the other hand, the extracts showed significant antinociceptive effect when tested in the hot plate model. The most active natural product as antinociceptive agent was hofmeisterin III (1) which also was the most stable in the stability study. Its pharmacological effect seems to be partially mediated by an opioid mechanism since naloxone inhibits its action. Using compound 1 as a lead molecule, several synthetic thymol esters were prepared and only compounds 13, 15 and 17 were antinoceptive at the dose of 1 mg/kg. CONCLUSIONS: The present investigation provided evidence of the efficacy of several preparations of Hofmeisteria schaffneri as antinociceptive agents. The most active preparation was the essential oil which contained large amount of hofmeisterin III (1) and other thymol derivatives. Some novel synthetic analogs of hofmeisterin III with antinociceptive properties were discovered. The nature of the ester chain of these analogs did not have a clear impact on the antinociceptive activity. The phyto-preparations analyzed in this study were not toxic to mice according to the Lorke's test; therefore considering their long term use of the plant they might be secure for human consumption"
Keywords:"Analgesics/pharmacology/*therapeutic use/toxicity Animals Asteraceae/*chemistry Hot Temperature Lethal Dose 50 Male Mice Mice, Inbred ICR Naloxone/pharmacology Narcotic Antagonists/pharmacology/*therapeutic use/toxicity Oils, Volatile/chemistry/pharmacolo;"
Notes:"MedlineAngeles-Lopez, Guadalupe Perez-Vasquez, Araceli Hernandez-Luis, Francisco Deciga-Campos, Myrna Bye, Robert Linares, Edelmira Mata, Rachel eng Research Support, Non-U.S. Gov't Ireland 2010/07/17 J Ethnopharmacol. 2010 Sep 15; 131(2):425-32. doi: 10.1016/j.jep.2010.07.009. Epub 2010 Jul 13"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 16-11-2024